EP0406902B1 - Liquid transfer article having a vapor deposited protective polymer film - Google Patents
Liquid transfer article having a vapor deposited protective polymer film Download PDFInfo
- Publication number
- EP0406902B1 EP0406902B1 EP90112969A EP90112969A EP0406902B1 EP 0406902 B1 EP0406902 B1 EP 0406902B1 EP 90112969 A EP90112969 A EP 90112969A EP 90112969 A EP90112969 A EP 90112969A EP 0406902 B1 EP0406902 B1 EP 0406902B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- wells
- liquid
- liquid transfer
- transfer article
- parylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 71
- 229920006254 polymer film Polymers 0.000 title 1
- 230000001681 protective effect Effects 0.000 title 1
- 229920000052 poly(p-xylylene) Polymers 0.000 claims abstract description 38
- 238000000576 coating method Methods 0.000 claims abstract description 33
- 239000011248 coating agent Substances 0.000 claims abstract description 26
- 239000000919 ceramic Substances 0.000 claims abstract description 19
- 239000000758 substrate Substances 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 14
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 9
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 9
- 238000000151 deposition Methods 0.000 claims description 7
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 150000001247 metal acetylides Chemical class 0.000 claims description 4
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 abstract description 11
- 239000000976 ink Substances 0.000 description 43
- 230000008569 process Effects 0.000 description 17
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 16
- 229910052802 copper Inorganic materials 0.000 description 16
- 239000010949 copper Substances 0.000 description 16
- 238000007639 printing Methods 0.000 description 15
- 239000010408 film Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 230000002209 hydrophobic effect Effects 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 238000010147 laser engraving Methods 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 239000010409 thin film Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 4
- 229910052721 tungsten Inorganic materials 0.000 description 4
- 239000010937 tungsten Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000005524 ceramic coating Methods 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 238000000197 pyrolysis Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 229910000531 Co alloy Inorganic materials 0.000 description 2
- 229910000684 Cobalt-chrome Inorganic materials 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- 229910018487 Ni—Cr Inorganic materials 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000007774 anilox coating Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000010952 cobalt-chrome Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000005474 detonation Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000001459 lithography Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- 229920002799 BoPET Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000006424 Flood reaction Methods 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 125000001743 benzylic group Chemical group 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 230000005226 mechanical processes and functions Effects 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- NRNFFDZCBYOZJY-UHFFFAOYSA-N p-quinodimethane Chemical group C=C1C=CC(=C)C=C1 NRNFFDZCBYOZJY-UHFFFAOYSA-N 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- CCEKAJIANROZEO-UHFFFAOYSA-N sulfluramid Chemical group CCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F CCEKAJIANROZEO-UHFFFAOYSA-N 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- MAKDTFFYCIMFQP-UHFFFAOYSA-N titanium tungsten Chemical compound [Ti].[W] MAKDTFFYCIMFQP-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41F—PRINTING MACHINES OR PRESSES
- B41F31/00—Inking arrangements or devices
- B41F31/26—Construction of inking rollers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N7/00—Shells for rollers of printing machines
- B41N7/06—Shells for rollers of printing machines for inking rollers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2207/00—Location or type of the layers in shells for rollers of printing machines
- B41N2207/02—Top layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N2207/00—Location or type of the layers in shells for rollers of printing machines
- B41N2207/10—Location or type of the layers in shells for rollers of printing machines characterised by inorganic compounds, e.g. pigments
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49544—Roller making
- Y10T29/4956—Fabricating and shaping roller work contacting surface element
- Y10T29/49563—Fabricating and shaping roller work contacting surface element with coating or casting about a core
Definitions
- the invention relates to a liquid transfer article for use in transferring a metered quantity of a liquid to another surface, said liquid transfer article comprising a substrate coated with ceramic or metallic carbide coatings having engraved in said coatings a pattern of wells adapted for receiving the metered quantity of liquid and wherein the microporosities in the surface of the wells are filled with a film of a vapor-deposited polymer.
- a liquid transfer article such as a roll, is used in the printing industry to transfer a specified amount of a liquid, such as ink or other substances, from the liquid transfer article to another surface.
- the liquid transfer article generally comprises a surface with a pattern of depressions or wells adapted for receiving a liquid and in which said pattern is transferred to another surface when contacted by the liquid transfer article.
- the wells are filled with the ink while the remaining surface of the article is wiped off. Since the ink is contained only in the pattern defined by the wells, it is this pattern that is transferred to another surface.
- a wiper or doctor blade is used to remove any excess liquid from the surface of the liquid transfer article. If the surface of the coated article is too coarse, excessive liquid, such as ink, will not be removed from the land area surface of the coarse article thereby resulting in the transfer of too much ink onto the receiving surface and/or onto the wrong place. Therefore, the surface of the liquid transfer article should be finished and the wells or depressions clearly defined so that they can accept the liquid.
- a gravure-type roll is commonly used as a liquid transfer roll.
- a gravure-type roll is also referred to as an applicator or pattern roll.
- a gravure roll is produced by cutting or engraving various sizes of wells into portions of the roll surface. These wells are filled with liquid and then the liquid is transferred to the receiving surface. The diameter and depth of the wells may be varied to control the volume of liquid transfer. It is the location of the wells that provides a pattern of the liquid to be transferred to the receiving surface while the land area defining the wells does not contain any liquid and therefore cannot transfer any liquid.
- the land area is at a common surface level, such that when liquid is applied to the surface and the liquid fills or floods the wells, excess liquid can be removed from the land area by wiping across the roll surface with a doctor blade.
- each well determines the amount of liquid which is transferred to the receiving surface.
- the depth and size of each well determines the amount of liquid which is transferred to the receiving surface.
- the liquid may be transferred to a receiving surface in a predetermined pattern to a high degree of precision having different print densities by having various depth and/or size of wells.
- a gravure roll is a metal roll with an outer layer of copper.
- the engraving techniques employed to engrave the copper are mechanical processes, e.g., using a diamond stylus to dig the well pattern, or photochemical processes that chemically etch the well pattern.
- the copper surface is usually plated with chrome. This last step is required to improve the wear life of the engraved copper surface of the roll. Without the chrome plating, the roll wears quickly, and is more easily corroded by the inks used in the printing. For this reason, without the chrome plating, the copper roll has an unacceptably low life.
- the life of the roll is often unacceptably short. This is due to the abrasive nature of the fluids and the scrapping action caused by the doctor blade.
- the rapid wear of the roll is compensated by providing an oversized roll with wells having oversized depths.
- this roll has the disadvantage of higher liquid transfer when the roll is new.
- the volume of liquid transferred to a receiving surface rapidly decreases thereby causing quality control problems.
- the rapid wear of the chrome-plated copper roll also results in considerable downtime and maintenance costs.
- Ceramic coatings have been used for many years on anilox rolls to give extremely long life.
- Anilox rolls are liquid transfer rolls which transfer a uniform liquid volume over the entire working surface of the rolls.
- Engraving of ceramic coated rolls cannot be done with conventional engraving methods used for engraving copper rolls; so these rolls must be engraved with a high energy beam, such as a laser or an electron beam.
- Laser engraving results in the formation of wells with a new recast surface about each well and above the original surface of the roll, such recast surface having an appearance of a miniature volcano crater about each well. This is caused by solidification of the molten material thrown from the surface when struck by the high energy beam. Thus the recast surface should be removed for most printing applications.
- the printing plate In offset printing the printing plate is not directly applied to the paper but first transfers its image to an offset blanket cylinder which is a flexographic surface, such as rubber, and the image is transferred from the blanket cylinder to the paper.
- Printing ink is applied to the plate cylinder by ink transfer or ink metering rolls which may be a single roll or may be a series of rolls.
- the image and non-image areas are on the same plane on the printing plate but the image area is grease-receptive and water-repellent whereas the non-image area is water-receptive and grease-repellent.
- the ink solvent therefore adheres only to the image areas, from which it is transferred to the surface to be printed, usually by the offset method.
- water or "fountain solution” is fed to the printing plate roll just before it contacts the ink transfer rolls. This is usually done by means of rollers which meter the amount of water applied.
- the moisture film produced on the printing plate roll is continuous on the non-image areas of the plate and acts as a barrier preventing adhesion of ink. Any moisture on the greasy image areas is discontinuous and does not prevent transfer of ink to them.
- the ink transfer or metering roll surface must be oleophilic so that it receives the greasy printing ink into the wells engraved on its surface and must also be hydrophobic so that it repels water which is on the surface of the printing roll.
- an ink transfer roll has been made with a pore-free surface of copper which has been found to be both oleophilic and hydrophobic.
- copper surfaces are relatively soft and are not hard wearing, and therefore the surface of the engraved copper roll generally has been coated with a layer of pore-free chromium to increase its resistance to wear. Such wear is particularly evident where doctor blades are used to meter the amount of ink transferred.
- the application of a doctor blade however does produce continuous wear on the surface of the transfer roll and much consideration has been given in the past to the production of ink transfer or ink metering rolls which are much more resistant to wear.
- German Patent Application DE 3713027 A1 discloses a liquid transfer roll having a multiplicity of wells and wherein the wells contain a moisture-repellant coating of a material such as vapor-deposited copper, nickel, silicon, asphalt or a suitable synthetic in the form of teflon or mylar.
- the invention relates to a liquid transfer article for use in transferring a metered quantity of a liquid to another surface comprising a substrate coated with a material selected from the group consisting of ceramics, and metallic carbides; a pattern of wells engraved in said coating with each of said wells having a surface adapted for receiving a metered quantity of a liquid; and wherein any microporosities in the surface of the wells are filled with vapor-deposited parylene and wherein the surface of the wells has a vapor-deposited film of parylene from 0.1 to 3 »m thick.
- the vapor-deposited parylene provides a thin film coating of the surface of the wells that exhibits oleophilic and hydrophobic characteristics.
- the invention also relates to a method for producing a liquid transfer article for use in transferring a metered quantity of a liquid to another surface comprising the steps:
- Parylene has the ability to provide ultra-thin films that can conform to substrates of varied geometrical shapes. This will enable the parylene to enter into not only the extremely small wells, but also fill any microporosities, e.g., cracks, fissures, pinholes or crevices, that generally form in the surface of the wells during the laser engraving process. Although the wells can be as small as 10 microns diameter and 2 microns height, the parylene can still fill any microporosities that may have been formed in the surface of the wells due to the laser engraving process. Vapor-deposited parylene provides a tough pinhole free film that can be deposited as thin as 0.10 micron and up to 100 microns.
- microporosities e.g., cracks, fissures, pinholes or crevices
- Parylene is a physically stable and chemically inert poly-crystalline material that is extremely resistant to chemical attack and insoluble in most known solvents. It provides excellent protection from moisture, corrosive vapors and other hostile environments. Vapor-deposited parylene also provides pinhole free coverage, microporosity penetration and purity in conformal coatings.
- Parylene is a generic term applied to the family of unsubstituted and substituted poly-p-xylylenes.
- the polymers can be homopolymers or copolymers depending on whether they are derived from one particular dimer or a mixture of different dimers.
- the unsubstituted homopolymer poly-p-xylylene has the structure: and substituted homopolymers may be illustrated by the following structures:
- the substituent can be any organic or inorganic group, which can normally be substituted on aromatic nuclei provided that the dimer and monomer are vaporizable under process conditions. Examples of substituents are the halogens, and cyano groups, e.g., cyanoparylene and dicyanoparylene. Fluorine atoms or other substituents can be substituted for the hydrogen atoms in the methylene groups, if desired.
- parylene A description of parylene, processes for making it, and the apparatus in which parylene deposition can be effected may be found in United States Patent Nos. 3,246,627; 3,301,707; and 3,600,216, all of which patents are incorporated herein by reference as if they were printed in their entirety. It will be observed, however, that the term "parylene” is not used in these patents. Instead, the term poly-p-xylylene is used generically and this term is considered to include both the unsubstituted and substituted varieties in the form of homopolymers or copolymers just as the term parylene does in this specification.
- the process for coating a substrate with parylene is conventional. Typical steps and conditions of such a process involve first vaporizing a cyclic dimer which contains the desired repeating unit, e.g., cyclic di-p-xylylene, at a pressure of about 13 to about 133 Pa (about 0.1 to about 1 Torr) temperature of about 150°C to about 200°C; then, pryolyzing the vaporized cyclic dimer at slightly lower pressure at about 670°C to about 690°C., the pyrolysis step breaking the benzylic carbon to carbon bonds to provide the p-xylylene monomer in the vapor state; and, finally, introducing the vaporous monomer into a deposition chamber containing the substrate, at still slightly lower pressure, but at ambient temperatures in the range of about 20°C to about 30°C, whereby the monomer condenses and polymerizes on all of the exposed surface of the substrate to provide a thin parylene film. There is a slight pressure gradient established throughout the process
- the apparatus used typically comprises a vaporized or sublimator section, a pyrolysis zone, and a deposition chamber, all connected by tubing, with the deposition chamber having a valved outlet connected to a pump for providing the required pressure. Heating means for vaporization and pyrolysis are provided while condensation is effected by ambient temperature.
- the thickness of the parylene film can be from 0.1 to 3 microns. For most applications of this invention, the thickness of the parylene film should be from 0.5 to 3 microns. Deposits of parylene less than 0.5 micron thick would not generally provide adequate protection for the surface of the wells to insure that the microporosities in the surface of the wells are filled and that the overall surface remains oleophilic and hydrophobic while a coating more than 10 microns thick could in some applications needlessly reduce the capacity of the wells for holding the liquid.
- the depth of the wells engraved in the surface of the ceramic is not usually more than about 20 microns and the thickness of the film of the vapor-deposited polymers should be as thin as possible, consistent with retention of the oleophilic and hydrophobic properties of the wells and filling the microporosities in the wells.
- coatings from about 0.5 micron to about 3 microns, preferably from about 1 micron to about 3 microns, in thickness are effective to achieve these purposes. Most preferably, a coating of about 1.5 micron would be suitable for most applications.
- the change in surface properties of the wells arises out of the absorption of water into the microporosities (fissures, cavities and pinholes) in the wells surface produced during the engraving process, such water being preferentially absorbed into the microporosities. Any absorbed water ultimately builds up to a point where it retards or prevents ink take-up by the wells, i.e., it changes the surface properties of the individual wells and causes what is termed "blinding" on the surface of the ink transfer roll. It is believed that the vapor-deposited polymer coating fills the microporosities in the wells' surface and prevents the absorption of water into such microporosities.
- the general process steps necessary in producing an ink roll according to the method of the present invention involve first grit blasting the surface of the metallic substrate roll usually of low carbon steel or copper, etc. and applying to the grit blasted surface a coating such as ceramic by thermally spraying the coating onto the surface.
- the coating is next ground so as to remove surface irregularities from the coating surface and is then engraved with a suitable pattern by a pulsed laser technique. Since the engraving process throws up a certain amount of recast at the edges of the wells produced by the laser beam pulses, the roll could be polished after engraving so as to provide a smooth surface which in some applications will involve contact with a doctor blade.
- the application of the vapor-deposited polymer can be carried out either before or after the final polishing, but is preferably carried out after the final polishing. Since the amount of polymer which is applied is very thin, it does not deleteriously affect the final surface which takes the doctor blade.
- any suitable coating such as a refractory oxide or metallic carbide coating, may be applied to the surface of the roll.
- tungsten carbide-cobalt, tungsten carbide-nickel, tungsten carbide-cobalt chromium, tungsten carbide-nickel chromium, chromium-nickel, aluminum oxide, chromium carbide-nickel chromium, chromium carbide-cobalt chromium, tungsten-titanium carbide-nickel, cobalt alloys, oxide dispersion in cobalt alloys, aluminum-titania, copper based alloys, chromium based alloys, chromium oxide, chromium oxide plus aluminum oxide, titanium oxide, titanium plus aluminum oxide, iron based alloys, oxide dispersed in iron based alloys, nickel and nickel based alloys, and the like may be used.
- the ceramic or metallic carbide coatings can be applied to the metal surface of the roll by either of two well known techniques; namely, the detonation gun (D-gun) process or the plasma coating process.
- the detonation gun process is well known and fully described in United States Patent Nos. 2,714,563; 4,173,685; and 4,519,840, the disclosures of which are hereby incorporated by reference as if they were printed in their entirety.
- Conventional plasma techniques for coating a substrate are described in United States Patent Nos. 3,016,447; 3,914,573; 3,958,097; 4,173,685; and 4,519,840, the disclosures of which are hereby incorporated by reference as if they were printed in their entirety.
- the thickness of the coating applied by either the plasma process or D-gun process can range from 0.013 to 2.54 mm (0.5 to 100 mils) and the roughness ranges from about 1.27 to 25.4 »m (about 50 to about 1000 micro-inches) R a depending on the process, i.e. D-gun or plasma, the type of coating material, and the thickness of the coating.
- R a is the average surface roughness measured in micro-inches by ANSI Method B46.1, 1978. In this measuring system, the higher the number, the rougher the surface.
- a wide variety of laser machines are available for forming wells in the ceramic or metallic carbide coatings.
- lasers capable of producing a beam or pulse of radiation of from 0.0001 to 0.4 joule per laser pulse for a duration of 10 to 300 microseconds can be used.
- the laser pulses can be separated by 30 to 2000 microseconds depending on the specific pattern of well desired. Higher or lower values of the energy and time periods can be employed and other laser-engraved techniques readily available in the art can be used for this invention.
- the roughness should typically range from 0.5 to 25.4 »m (20 to 1000 micro-inches) R a and the wells can range from 10 microns to 300 microns diameter and from 2 microns to 250 microns height.
- the liquid that can be transferred to a receiving surface is any liquid such as ink, liquid adhesives and the like.
- an ink transfer roll generally designated as 1, comprises a cylinder 2 composed of a substrate 3 of low carbon steel, the surface of which has been grit blasted to provide a roughened surface 4.
- a ceramic coating 5 (preferably chromium oxide) 75 to 100 microns thick over lays the grit blasted surface 4 having been applied thereto by thermal spraying.
- the surface of the ceramic layer 5 is formed by grinding, laser beam engraving and polishing into a pattern of wells 6 for receiving ink, the surface areas 7 between the wells being polished to take a doctor blade (not shown).
- the surface of the wells 6 and polished surface areas 7 is coated with a film of parylene, preferably about 1.5 micron thick.
- the coated layer 5 can be applied by conventional techniques followed by conventional grinding to provide a surface of less than 0.5 micro meter R a .
- the polished engraved surface of this invention can then be coated with a film of parylene by conventional vapor-deposition techniques referred to above.
- the surface to be coated with parylene can be degreased at 48°C using a chlorindated solvent and ultrasonic vibration, the degreasing being carried out in three steps using fresh chlorinated solvent at each step.
- the surface is then soaked in an isopropanol/ deionized water mixture and then dipped into a promotion system composed of UCAR-A174 (UCAR is a Registered Trademark of Union Carbide) in an isopropanol/deionized water mixture.
- UCAR-A174 a Registered Trademark of Union Carbide
- the parylene can then be vapor-deposited by conventional means to produce a film 1.5 micron thick.
- the vapor-deposited parylene will effectively fill any microporosities on the surface of the wells of the laser engraved roll while also depositing a thin film of parylene on the surface of the wells.
- the ink transfer roll is then ready for use in an offset printed apparatus.
- Figure 3 shows an enlarged photograph of the surface of a well of a laser engraved roll while Figure 4 shows an even larger photograph of the central area of the surface of the well shown in Figure 3.
- microporosities such as cavities 30 and cracks 32 are formed in the surface of the wells during the laser engraved process.
- some of the crystals of the ceramic coating are cracked producing crevices and fissures in the surface of the wells.
- the vapor-deposited parylene will fill these microporosities and deposit an extremely thin uniform film on the surface of the wells that will prevent the absorption of water into such microporosities.
- the thin film of parylene exhibits oleophilic and hydrophobic characteristics which makes it ideally suited for liquid transfer applications.
Landscapes
- Inking, Control Or Cleaning Of Printing Machines (AREA)
- Laminated Bodies (AREA)
- Decoration By Transfer Pictures (AREA)
- Coating Apparatus (AREA)
- Physical Vapour Deposition (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Shaping Of Tube Ends By Bending Or Straightening (AREA)
- Peptides Or Proteins (AREA)
- Polymerisation Methods In General (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US376524 | 1989-07-07 | ||
US07/376,524 US4960050A (en) | 1989-07-07 | 1989-07-07 | Liquid transfer article having a vapor deposited protective parylene film |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0406902A2 EP0406902A2 (en) | 1991-01-09 |
EP0406902A3 EP0406902A3 (en) | 1992-06-10 |
EP0406902B1 true EP0406902B1 (en) | 1995-03-01 |
Family
ID=23485360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90112969A Expired - Lifetime EP0406902B1 (en) | 1989-07-07 | 1990-07-06 | Liquid transfer article having a vapor deposited protective polymer film |
Country Status (12)
Country | Link |
---|---|
US (1) | US4960050A (el) |
EP (1) | EP0406902B1 (el) |
JP (1) | JP2517453B2 (el) |
KR (1) | KR960003334B1 (el) |
AT (1) | ATE119104T1 (el) |
AU (1) | AU628764B2 (el) |
CA (1) | CA2020565C (el) |
DE (1) | DE69017289T2 (el) |
ES (1) | ES2068949T3 (el) |
FI (1) | FI903442A0 (el) |
GR (1) | GR3015258T3 (el) |
SG (1) | SG67285G (el) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5207158A (en) * | 1991-02-19 | 1993-05-04 | Rockwell International | Long lived, variable-delivery ink metering method, system and roller for keyless lithography |
US5647279A (en) * | 1992-09-05 | 1997-07-15 | Heidelberger Druckmaschinen Ag | Printing machine roller and method of production thereof |
DE4229700C2 (de) * | 1992-09-05 | 1997-02-13 | Heidelberger Druckmasch Ag | Feuchtwerkswalze für eine Druckmaschine sowie Verfahren zu ihrer Beschichtung |
DE69326209T2 (de) * | 1992-10-16 | 2000-04-13 | Canon K.K., Tokio/Tokyo | Bilderzeugungsgerät |
JPH08224878A (ja) * | 1994-11-21 | 1996-09-03 | Lexmark Internatl Inc | インク・ジェット印刷用のノズル・プレート |
DE19515393B4 (de) * | 1995-04-26 | 2004-01-15 | Man Roland Druckmaschinen Ag | Bedruckstofführende Oberflächenstruktur, vorzugsweise für Druckmaschinenzylinder oder deren Aufzüge |
US6849295B2 (en) * | 1996-08-22 | 2005-02-01 | Vacuumschmelze Gmbh | Method for producing a winding protection for tape-wound cores |
US6109719A (en) * | 1998-06-03 | 2000-08-29 | Lexmark International, Inc. | Printhead thermal compensation method and apparatus |
GB9828305D0 (en) * | 1998-12-23 | 1999-02-17 | Eastman Kodak Co | Device to reduce electrostatic pattern transfer in coating processes |
SE0000215L (sv) * | 2000-01-25 | 2001-07-26 | Btg Eclepens Sa | Rakelknive |
WO2001076811A1 (en) * | 2000-04-07 | 2001-10-18 | Whyco Technologies, Inc. | Method of masking coatings and resultant object |
US6290834B1 (en) | 2000-04-12 | 2001-09-18 | Ceramic Coatings Technologies, Inc. | Ceramic coated liquid transfer rolls and methods of making them |
KR100411835B1 (ko) * | 2001-01-19 | 2003-12-18 | 유피씨(주) | 통기성 합지 제조시스템, 제조 방법 및 그 통기성 합지 |
EP1393820A3 (en) * | 2002-06-28 | 2004-11-03 | Eastman Kodak Company | Roller coating |
ATE414732T1 (de) * | 2004-09-13 | 2008-12-15 | Asahi Kasei Chemicals Corp | Verfahren zur herstellung eines gehärteten produkts aus lichtempfindlichem harz |
JP5085030B2 (ja) * | 2004-12-24 | 2012-11-28 | 東海ゴム工業株式会社 | 現像ロールおよびその製法 |
DE102005030918A1 (de) * | 2005-06-30 | 2007-01-04 | Man Roland Druckmaschinen Ag | Farbduktorwalze einer Rollendruckmaschine |
US20070057432A1 (en) * | 2005-09-12 | 2007-03-15 | Yanmo Enterprise Co., Ltd. | Roller with spray-coated surface structure |
US20070057431A1 (en) * | 2005-09-12 | 2007-03-15 | Yanmo Enterprise Co., Ltd. | Roller with surface friction |
WO2008016373A2 (en) * | 2005-12-22 | 2008-02-07 | The Penn State Research Foundation | Method and systems for forming and using nanoengineered sculptured thin films |
US20070177119A1 (en) * | 2006-02-02 | 2007-08-02 | Keiko Chiba | Exposure apparatus and device manufacturing method |
EP1905868B1 (de) * | 2006-09-29 | 2012-11-07 | Koenig & Bauer Aktiengesellschaft | Verfahren zur Herstellung einer anti-adhäsiven und verschleißbeständigen Oberfläche |
US8535805B2 (en) * | 2008-04-28 | 2013-09-17 | The United States Of America, As Represented By The Secretary Of The Navy | Hydrophobic nanostructured thin films |
US20100015354A1 (en) * | 2008-07-16 | 2010-01-21 | Lee Tai-Cheung | Method of making rollers with a fine pattern |
DE102008059757A1 (de) * | 2008-12-01 | 2010-06-02 | Tesa Se | Verfahren zum Markieren oder Beschriften eines Werkstücks |
KR101066980B1 (ko) | 2010-04-01 | 2011-09-22 | 주식회사 누리텍 | 스테인레스 배관의 부식 방지를 위한 패럴린 코팅방법 |
CN101817252B (zh) * | 2010-04-08 | 2012-01-25 | 云南侨通包装印刷有限公司 | 一种陶瓷网纹窜水辊及制作方法 |
JP5387623B2 (ja) * | 2011-06-17 | 2014-01-15 | トヨタ自動車株式会社 | 塗工ローラの製造方法及び塗工ローラ |
EP2910506B1 (en) * | 2012-10-19 | 2018-07-18 | Sato Holdings Kabushiki Kaisha | Elastic body roller |
CN104442139A (zh) * | 2013-09-13 | 2015-03-25 | 李大章 | 具有湾流图案的转印轮具的制造方法 |
WO2016126230A1 (en) * | 2015-02-02 | 2016-08-11 | Eastman Kodak Company | Anilox roll with low surface energy zone |
US9522524B2 (en) | 2015-02-02 | 2016-12-20 | Eastman Kodak Company | Method of multi-station flexographic printing including anilox roll with low surface energy zone |
JP2019059209A (ja) * | 2017-09-28 | 2019-04-18 | 大日本印刷株式会社 | 離型性に優れたヒートシール性積層体、及び該積層体からなる包装材料、包装袋 |
US11059147B2 (en) | 2018-03-30 | 2021-07-13 | Saint-Gobain Abrasives, Inc./Saint-Gobain Abrasifs | Abrasive article including a coating |
JP7139443B2 (ja) | 2018-03-30 | 2022-09-20 | サンーゴバン アブレイシブズ,インコーポレイティド | コーティングを含む接着研磨物品 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4301730A (en) * | 1977-09-29 | 1981-11-24 | Pamarco Incorporated | Anilox roll and method of making the same |
US4173664A (en) * | 1978-01-20 | 1979-11-06 | Union Carbide Corporation | Parylene stabilization |
GB2049102A (en) * | 1979-05-03 | 1980-12-17 | Csi Corp | Transfer roll |
DE3316348C2 (de) * | 1983-05-05 | 1985-03-07 | PTG Plasma-Oberflächentechnik GmbH, 7240 Horb | Verfahren zum Beschichten eines Werkstückes |
JPS6044394A (ja) * | 1983-08-22 | 1985-03-09 | Mitsubishi Heavy Ind Ltd | インキロ−ラ |
US4567827A (en) * | 1985-02-04 | 1986-02-04 | Rockwell International Corporation | Copper and nickel layered ink metering roller |
US4601242A (en) * | 1985-02-04 | 1986-07-22 | Rockwell International Corporation | Copper and ceramic composite ink metering roller |
JPS62275783A (ja) * | 1986-05-24 | 1987-11-30 | Tokyo Kikai Seisakusho Ltd | メッシュロ−ルおよびメッシュロ−ルの製造方法 |
DE3713027A1 (de) * | 1987-04-16 | 1988-11-17 | Frankenthal Ag Albert | Rasterwalze fuer ein offsetfarbwerk, sowie verfahren zur herstellung einer derartigen rasterwalze |
-
1989
- 1989-07-07 US US07/376,524 patent/US4960050A/en not_active Expired - Lifetime
-
1990
- 1990-07-06 EP EP90112969A patent/EP0406902B1/en not_active Expired - Lifetime
- 1990-07-06 JP JP2177605A patent/JP2517453B2/ja not_active Expired - Fee Related
- 1990-07-06 KR KR1019900010232A patent/KR960003334B1/ko not_active IP Right Cessation
- 1990-07-06 AU AU58720/90A patent/AU628764B2/en not_active Ceased
- 1990-07-06 SG SG1995906285A patent/SG67285G/en unknown
- 1990-07-06 AT AT90112969T patent/ATE119104T1/de not_active IP Right Cessation
- 1990-07-06 DE DE69017289T patent/DE69017289T2/de not_active Expired - Fee Related
- 1990-07-06 CA CA002020565A patent/CA2020565C/en not_active Expired - Lifetime
- 1990-07-06 ES ES90112969T patent/ES2068949T3/es not_active Expired - Lifetime
- 1990-07-06 FI FI903442A patent/FI903442A0/fi not_active IP Right Cessation
-
1995
- 1995-03-02 GR GR950400325T patent/GR3015258T3/el unknown
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 09, no. 137 (P-363) 31 May 1985; JP A 60 018 749 (MARATA SEISAKSHO) 11.07.1983 * |
Also Published As
Publication number | Publication date |
---|---|
ATE119104T1 (de) | 1995-03-15 |
AU5872090A (en) | 1991-01-10 |
FI903442A0 (fi) | 1990-07-06 |
GR3015258T3 (en) | 1995-06-30 |
KR960003334B1 (ko) | 1996-03-08 |
DE69017289T2 (de) | 1995-10-19 |
CA2020565C (en) | 1999-01-19 |
ES2068949T3 (es) | 1995-05-01 |
JPH03150195A (ja) | 1991-06-26 |
JP2517453B2 (ja) | 1996-07-24 |
EP0406902A3 (en) | 1992-06-10 |
US4960050A (en) | 1990-10-02 |
SG67285G (en) | 1995-09-01 |
KR910003146A (ko) | 1991-02-27 |
DE69017289D1 (de) | 1995-04-06 |
CA2020565A1 (en) | 1991-01-08 |
EP0406902A2 (en) | 1991-01-09 |
AU628764B2 (en) | 1992-09-17 |
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